FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

OPERATION ROOM TOWEL

K Number: K881479 · Decision Apr 14, 1988
Classifications
1
FEI Numbers
200
Registration Numbers
200
Same Product Code
449
Applicant Total
3
Review Days
7

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Basic Information

Device Name
OPERATION ROOM TOWEL
K Number
K881479
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Rahn Laboratories
Date Received
April 7, 1988
Decision Date
April 14, 1988
Product Code
KKX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KKX Drape, Surgical, Antimicrobial

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